Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP268624.RADhTs2gtpXGGCoViYsvt_WiqyJ_7li55H3MViWz0bInI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP268624.RADhTs2gtpXGGCoViYsvt_WiqyJ_7li55H3MViWz0bInI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP268624.RADhTs2gtpXGGCoViYsvt_WiqyJ_7li55H3MViWz0bInI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP268624.RADhTs2gtpXGGCoViYsvt_WiqyJ_7li55H3MViWz0bInI130_provenance.
- NP268624.RADhTs2gtpXGGCoViYsvt_WiqyJ_7li55H3MViWz0bInI130_assertion description "[Our study illustrates that if only a single heterozygous SLC26A4/PDS mutation is found in a patient with goiter and deafness, other genetic explanations should be considered.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP268624.RADhTs2gtpXGGCoViYsvt_WiqyJ_7li55H3MViWz0bInI130_provenance.
- NP268624.RADhTs2gtpXGGCoViYsvt_WiqyJ_7li55H3MViWz0bInI130_assertion evidence source_evidence_literature NP268624.RADhTs2gtpXGGCoViYsvt_WiqyJ_7li55H3MViWz0bInI130_provenance.
- NP268624.RADhTs2gtpXGGCoViYsvt_WiqyJ_7li55H3MViWz0bInI130_assertion SIO_000772 16684826 NP268624.RADhTs2gtpXGGCoViYsvt_WiqyJ_7li55H3MViWz0bInI130_provenance.
- NP268624.RADhTs2gtpXGGCoViYsvt_WiqyJ_7li55H3MViWz0bInI130_assertion wasDerivedFrom befree-20140225 NP268624.RADhTs2gtpXGGCoViYsvt_WiqyJ_7li55H3MViWz0bInI130_provenance.
- NP268624.RADhTs2gtpXGGCoViYsvt_WiqyJ_7li55H3MViWz0bInI130_assertion wasGeneratedBy ECO_0000203 NP268624.RADhTs2gtpXGGCoViYsvt_WiqyJ_7li55H3MViWz0bInI130_provenance.
- befree-20140225 importedOn "2014-02-25" NP268624.RADhTs2gtpXGGCoViYsvt_WiqyJ_7li55H3MViWz0bInI130_provenance.